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Gerstmann syndrome

Gerstmann syndrome is a neurological disorder characterized by four primary symptoms: more...

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  1. Dysgraphia/agraphia
  2. Dyscalculia/acalculia
  3. Finger agnosia
  4. Left-right disorientation

In adults, the syndrome may occur after a stroke or in association with damage to the parietal lobe. In addition to exhibiting the above symptoms, many adults also experience aphasia, which is a difficulty in expressing oneself when speaking, in understanding speech, or in reading and writing.

There are few reports of the syndrome, sometimes called developmental Gerstmann syndrome, in children. The cause is not known. Most cases are identified when children reach school age, a time when they are challenged with writing and math exercises. Generally, children with the disorder exhibit poor handwriting and spelling skills, and difficulty with math functions, including adding, subtracting, multiplying, and dividing. An inability to differentiate right from left and to discriminate among individual fingers may also be apparent. In addition to the four primary symptoms, many children also suffer from constructional apraxia, an inability to copy simple drawings. Frequently, there is also an impairment in reading. Children with a high level of intellectual functioning as well as those with brain damage may be affected with the disorder.

There is no cure for Gerstmann syndrome. Treatment is symptomatic and supportive. Occupational and speech therapies may help diminish the dysgraphia and apraxia. In addition, calculators and word processors may help school children cope with the symptoms of the disorder.

In adults, many of the symptoms diminish over time. Although it has been suggested that in children symptoms may diminish over time, it appears likely that most children probably do not overcome their deficits, but learn to adjust to them.

The National Institute of Neurological Disorders and Stroke (NINDS) supports research on disorders that result from damage to the brain such as dysgraphia. The NINDS and other components of the National Institutes of Health also support research on learning disabilities. Current research avenues focus on developing techniques to diagnose and treat learning disabilities and increase understanding of the biological basis of them.

This disorder is often associated with brain lesions in the dominant (usually left) side of the angular and supramarginal gyri near the temporal and parietal lobe junction.

It should not be confused with Gerstmann-Straussler syndrome, which is a transmissible spongiform encephalopathy.


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Hearing loss as the initial presentation of Creutzfeldt-Jakob disease
From Ear, Nose & Throat Journal, 8/1/04 by Priya Krishna


Creutzfeldt-Jakob disease is a rare type of spongiform encephalopathy. Affected patients present with constitutional symptoms, which progress to severe mental deterioration and movement disorders. Dizziness is the most common early otologic symptom. Few reports in the literature describe patients with Creutzfeldt-Jakob disease who present with sudden-onset hearing loss as their primary symptom for seeking treatment. This paper discusses one such patient and reviews the clinical presentation, treatment options, and relevant literature.


Prion-associated encephalopathies are characterized by requiting a protein component (prion) for communicability. One such encephalopathy, Creutzfeldt-Jakob disease (CJD), has been recognized for more than a century. However, few reports in the literature describe patients who first present with otolaryngologic symptoms and signs. This prodromal complex may include symptoms such as dizziness or hearing loss in addition to the more commonly associated signs of progressive dementia, visual field defects, and ataxia. (1)

With this vague clinical picture, CJD can cause considerable diagnostic perplexity. In this article, we describe one patient with CJD who first presented with otolaryngologic symptoms and review the literature on this subject.

Case report

A 74-year-old woman presented to the otolaryngology clinic with a history of sudden-onset, right-sided hearing loss of 2 weeks' duration. Her history also included symptoms of sudden memory loss, ataxia, and diplopia. A poor historian, the patient was accompanied by a brother and sister who provided the history. Prior to her current illness, she lived independently. The patient's siblings were unaware of any history of vertigo or prior occurrence of similar symptoms. The patient developed progressive imbalance and had fallen three times in the 2 weeks prior to presentation. Her family also noted that she had scanning speech. The presumptive diagnosis after evaluation in a local urgent care department was Meniere's disease. The patient's past medical history was unremarkable except for abdominal lysis of adhesions and cataract surgery.

On physical examination, the patient exhibited poor eye tracking, shuffling gait, and truncal ataxia with intention tremor. Audiometric testing (figure 1) revealed moderate-to-severe bilateral sensorineural hearing loss with poorer word recognition than would be predicted by the degree of hearing loss.


The patient was admitted for further evaluation with a possible diagnosis of cerebrovascular accident. Several blood tests (erythrocyte sedimentation rate, angiotensin-converting enzyme I levels, Lyme titer, folate, vitamin [B.sub.12], ceruloplasmin, CSF analysis, thyroid panel, CHEM-7, and CBC) were ordered, all of which were negative or within normal limits. Magnetic resonance imaging of the brain (figure 2) indicated some periventricular white matter change; magnetic resonance angiography and carotid ultrasound were normal. In the first 2 weeks after her admission, the patient began to develop involuntary jerking of the upper extremities and increased tremor and startle myoclonus. Her symptoms continued to progress, and she developed aphasia and apraxia. An auditory brainstem response test was attempted, but waveforms were not reproducible. Electroencephalography was nonspecific, with background slowing and occasional triphasic waves (figure 3), indicating a global encephalopathy with lack of periodicity. A right frontal brain biopsy confirmed CJD by Western blot analysis with the presence of protease-resistant prion protein.


Following the initial workup, the patient was admitted to a rehabilitation unit to begin physical therapy. The patient's dementia and level of consciousness deteriorated rapidly, and she expired less than 2 months from her original date of admission.


Creutzfeldt-Jakob disease is a rare disorder of transmissible spongiform encephalopathy characterized by progressive dementia. It is a prion disease requiring a protein component (prion) for transmissibility, similar to kuru, bovine spongiform encephalopathy (mad cow disease), and scrapie. Creutzfeldt and Jakob, independently, first described the disease. The first published description was of a 22-year-old woman with a 1-year history of progressive dementia, spasticity, ataxia, and startle myoclonus. (2) Simultaneously, Jakob identified 3 patients with a unique syndrome. (3-5) All were older than Creutzfeldt's patient and demonstrated a destructive process in the cerebral cortex, especially in the rolandic region, caudate, putamen, and thalamus. The first name for this disease was "spastic pseudosclerosis" because of its similarity to other diseases, such as multiple sclerosis and amyotrophic lateral sclerosis. A family with the disease was then described in the early to mid-1900s in which 11 members of the family had died of the same process. (6)

Multiple forms of CJD have been recognized. The first is the typical form, otherwise known as subacute spongiform encephalopathy. Variants are described on the basis of localization of the disease process and presenting symptoms. Familial fatal insomnia involves the thalamus, and Heidenhain's variant involves the occipital lobes. Related prion disorders include Gerstmann-Straussler-Scheinker syndrome, which is marked by cerebellar ataxia; and prion protein (PrP) and atypical forms of CJD caused by other mutations of the PrP gene (PRNP). (6)

The typical form of CJD has a mean age at onset of 60 [+ or -] 9 years. This is in contrast to Alzheimer's disease, the incidence of which increases markedly after age 60. There is no reported sex predilection for the disease. The annual incidence is 0.5 to 2 cases per million. (1,7) Approximately 15% of cases are familial, caused by a mutation on the gene encoding the PrP, and are transmitted in an autosomal dominant pattern. (6) Penetrance in familial cases also increases with age. Although 60% of familial mutations of the PRNP involve codon 200, multiple codons may be involved in members of the same family, as well as in variants of CJD. (6) Most cases are sporadic, but iatrogenic causes have been highly publicized. These include transmission via human cadaveric pituitary growth hormone, (8) corneal transplants, dural grafts, and EEG depth electrodes. (1) The iatrogenic cases involving pituitary hormone occurred in patients younger than 40 years of age, serving to differentiate them from sporadic cases. (8)

One third of patients experience prodromal constitutional symptoms, such as changes in sleeping and eating patterns and asthenia. Up to one fifth of the patients have a sudden onset of neurologic symptoms. (9) Dizziness is the most common otologic symptom noted. To date, only two other English-language reports of deafness as the primary presenting syndrome are published. (1,10) Tobias et al reported a patient with a progressive bilateral hearing loss that was cortical in origin, as indicated by phonologic errors consistent with abnormalities in central language processing. (10) In the second case, the patient presented with aural fullness and change in hearing. (1) Our patient had a progressive increase in baseline hearing loss with dysequilibrium but no vertigo. Patients with this constellation of symptoms may be diagnosed initially with a peripheral vestibulocochlear disorder, as in the case of our patient. Other early symptoms are visuospatial or cerebellar in origin, such as visual field defects, diplopia, and ataxia. (1,9)

Audiometric testing in these patients may reveal a poor word discrimination score that is out of proportion with the pure-tone hearing deficit. The role of imaging in the diagnosis of CJD is controversial. Computed tomography demonstrates volume loss in white matter and cortical atrophy with ventricular enlargement. In later stages of the disease, subdural fluid collections may be present. MRI, especially using higher-strength magnetic fields, may show high signals on T2 images in areas corresponding to the pathologic process, such as the basal ganglia, cortex, and periventricular white matter. Narrow-window techniques may increase the sensitivity for detecting early stages of CJD. (11) Single photon emission computed tomography (SPECT) has revealed cerebral perfusion deficits in CJD that may be used to differentiate it from other dementias, such as Alzheimer's disease. The correlation of SPECT scanning with the pathologic process behind CJD remains to be studied. (12)

CJD progresses relentlessly as patients develop further mental deterioration and movement disorders, such as chorea and myoclonus. Seizures may occur, and electroencephalographic testing is performed to assist in diagnosis. (9) More than 90% of patients in one series had findings of myoclonus, characteristic periodic sharp wave complexes (PSWCs), or both. (9) The accuracy of these PSWCs is debatable, with one series reporting a sensitivity of 67% and a somewhat higher specificity of 86%. Serial EEGs are recommended to help increase sensitivity. (13)

The ultimate diagnosis of CJD depends on neuropathologic findings in correlation with clinical history. A classic triad of spongiform change, neuronal loss, and astrocytosis has been well described (figure 4). However, spongiform change itself remains nonspecific; the only consistent location is in the head of the caudate nucleus. Spongiform change may also be absent in patients with a long duration of the disease. (14) PrP immunoreactivity may be performed for confirmation but may not distinguish typical CJD from clinical variants, (15) and only 10% of typical cases of CJD actually contain these PrP-positive amyloid plaques. (6)


CJD has a dismal outcome. Eighty percent of patients die within 1 year of onset, with the rest following a more chronic course. (6) Japanese forms of CJD have a much longer duration, with patients living beyond 4 years. (16) Little progress has been made in the search for treatment. Despite its rarity, it is important to be aware of this disease because of its significant diagnostic confusion.


(1.) Bigelow DC, Eisen MD, Yen DM, et al. Otolaryngological manifestations of Creutzfeldt-Jakob disease: Arch Otolaryngol Head Neck Surg 1998;124:707-10.

(2.) Creutzfeldt HG. Uber eine eigenartige herdformige Erkrankung des Zentralnervensystems. Vorlaufige Mitteilung. Zeitschrift fur die gesamte Neurologie und Psychiatrie 1920;57:1-18.

(3.) Jakob A. Uber eigenartige Erkrankungen des Zentralnervensystems mit bemerkenswertem anatomischem Befunde (spastische Pseudosklerose-Encephalomyelopathie mit disseminierten Degenerationsherden). Vorlaufige Mitteilung. Deutsche Zeitschrift fur Nervenheilkunde 1921;70:132-46.

(4.) Jakob A. Uber eigenartige Erkrankungen des Zentralnervensystems mit bemerkenswertem anatomischem Befunde (spastische Pseudosklerose-Encephalomyelopathie mit disseminierten Degenerationsherden). Zeitschrift fur die gesamte Neurologie und Psychiatrie 1921;64:147-228.

(5.) Jakob A. Uber eine der multiplen Sclerose klinisch nahestehende Erkrankung des Zentralnervensystems (spastische Pseudosklerose) mit bemerkenswertem anatomischem Befunde. Mitteilung eines vierten Falles. Med Klin 1921;17:372-6.

(6.) Richardson EP, Jr., Masters CL. The nosology of Creutzfeldt-Jakob disease and conditions related to the accumulation of [PrP.sup.CID] in the nervous system. Brain Pathol 1995;5:33-41.

(7.) Manolidis LS, Balojannis SJ. Ultrastructural alterations of the vestibular nuclei in Jakob-Creutzfeld disease. Acta Otolaryngol 1983;95:508-21.

(8.) Brown P, Gajdusek DC, Gibbs CJ, Jr., Asher DM. Potential epidemic of Creutzfeldt-Jakob disease from human growth hormone therapy. N Engl J Med 1985;313:728-31.

(9.) Brown P, Cathala F, Castaigne P, Gajdusek DC. Creutzfeldt-Jakob disease: Clinical analysis of a consecutive series of 230 neuropathologically verified cases. Ann Neurol 1986;20:597-602.

(10.) Tobias E, Mann C, Bone I, et al. A case of Creutzfeldt-Jakob disease presenting with cortical deafness (letter). J Neurol Neurosurg Psych 1994;57:872-3.

(11.) Garcia Santos JM, Lopez Corbalan JA, Martinez-Lage JF, Sicilia Guillen J. CT and MRI in iatrogenic and sporadic Creutzfeldt-Jakob Disease: As far as imaging perceives. Neuroradiology 1996;38: 226-31.

(12.) Aharon-Peretz J, Peretz A, Hemli JA, et al. SPECT diagnosis of Creutzfeld-Jacob disease. J Nucl Med 1995;36:616-17.

(13.) Steinhoff BJ, Racker S, Herrendorf G, et al. Accuracy and reliability of periodic sharp wave complexes in Creutzfeldt-Jakob Disease. Arch Neurol 1996;53:162-6.

(14.) Masters CL, Richardson EP, Jr. Subacute spongiform encephalopathy (Creutzfeldt-Jakob Disease). The nature and progression of spongiform change. Brain 1978;101:333-44.

(15.) Budka H, Aguzzi A, Brown P, et al. Neuropathological diagnostic criteria for Creutzfeldt-Jakob disease (CJD) and other human spongiform encephalopathies (prion diseases). Brain Pathol 1995;5: 459-66.

(16.) Yagashita S, Iwabuchi K, Amano N, Yokoi S. Further observation of Japanese Creutzfeldt-Jacob disease with widespread amyloid plaques. J Neurol 1989;236:145-8.

From the Division of Otolaryngology, Southern Illinois University School of Medicine, Springfield.

Reprint requests: Priya Krishna, MD, Division of Otolaryngology, St. John's Pavilion, Mail Code 9662, 301 N. 8th Street, Springfield, IL 62794-9662. Phone: (217) 545-4777; fax: (217) 545-0253; e-mail:

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